{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-21",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "68062-9001",
      "generic_name": "titanium dioxide, zinc oxide",
      "labeler_name": "Spa de Soleil",
      "brand_name": "Moisture Sunscreen SPF 50",
      "active_ingredients": [
        {
          "name": "ZINC OXIDE",
          "strength": "12.6 mg/120mL"
        },
        {
          "name": "OCTINOXATE",
          "strength": "9 mg/120mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "68062-9001-1",
          "description": "120 mL in 1 TUBE (68062-9001-1)",
          "marketing_start_date": "20210909",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Spa de Soleil"
        ],
        "spl_set_id": [
          "cb95975f-060d-23c2-e053-2a95a90adf1b"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "SOI2LOH54Z",
          "4Y5P7MUD51"
        ]
      },
      "marketing_category": "OTC MONOGRAPH DRUG",
      "dosage_form": "LOTION",
      "spl_id": "50b709f4-020b-4c97-e063-6294a90af7c8",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "TOPICAL"
      ],
      "marketing_start_date": "20210909",
      "product_id": "68062-9001_50b709f4-020b-4c97-e063-6294a90af7c8",
      "application_number": "M020",
      "brand_name_base": "Moisture Sunscreen SPF 50"
    }
  ]
}